Disease

Otosclerosis

About the Disease
Otosclerosis, also known as otospongiosis, is related to bone resorption disease and ankylosis, and has symptoms including earache An important gene associated with Otosclerosis is OTSC2 (Otosclerosis 2), and among its related pathways/superpathways are Phospholipase-C Pathway and Extracellular matrix organization. The drugs Acetylcysteine and Anti-Infective Agents have been mentioned in the context of this disorder. Affiliated tissues include bone, adrenal cortex and cortex, and related phenotypes are limbs/digits/tail and digestive/alimentary

Common Targets
COL1A1 | BMP4 | PPP2R5B | BMP2 | MMP2 | MEPE | TGFB1 | FOXL1 | FGF2 | RELN | Parathyroid Hormone Receptors (PTHR) (nonspecified subtype) | SERPINF1

疾病靶点研报
Otosclerosis

Note: If you'd like to get a target analysis report for Otosclerosis, or if you are interested to learn how our AI-powered BDE-Chem can design therapeutic molecules to interact with the target(s) above against the disease of Otosclerosis at a cost 90% lower than traditional approaches, please feel free to contact us at BD@silexon.ai.

Other Diseases

Epidermolysis Bullosa Simplex, Localized | Pigment Dispersion Syndrome | Tuberculous Meningitis | Cryptosporidiosis | Hemochromatosis | Gilbert Syndrome | Ganglioneuroma | Alkaptonuria | Prurigo Nodularis | Thrombocythemia, Essential | Spinal And Bulbar Muscular Atrophy | Congenital Disorders Of Glycosylation | Heroin Dependence | Non-Langerhans Cell Histiocytosis | Sialidosis | Neuroectodermal Tumors, Primitive | Fibrillation, Atrial | Cholangiocarcinoma | Parkinson's Disease | Thymoma, Malignant | Tracheal Disorders | Paraganglioma, Carotid Body | Martsolf Syndrome | Skin Fragility-woolly Hair Syndrome | Osteopetrosis | Cystitis | Anal Fissure | 6-pyruvoyl-tetrahydropterin Synthase Deficiency | Cat Eye Syndrome | Fetal Alcohol Syndrome | Hyperphosphatasia With Intellectual Disability Syndrome 4 | Feingold Syndrome | Chronic Enteropathy Associated With SLCO2A1 Gene | Filariasis | Donnai-Barrow Syndrome | Fibromyalgia | VEXAS Syndrome | Cancer, Breast | Oculocutaneous Albinism Type 2 | Meningococcal Meningitis | Kabuki Syndrome | Epidermolysis Bullosa Simplex | Spasticity | Infertility | Gastritis, Atrophic | Beckwith-Wiedemann Syndrome | Bursitis | Hemolytic Anemia | Benign Familial Pemphigus | Erythromelalgia | Syncope | Multiple Epiphyseal Dysplasia | Acrodermatitis | Atelosteogenesis Type 2 | Temtamy Preaxial Brachydactyly Syndrome | Hyperparathyroidism, Secondary | Chondrodysplasia Punctata 2, X-linked Dominant | Spinocerebellar Ataxia Type 23 | Pelizaeus-Merzbacher Disease | Infantile Neuroaxonal Dystrophy | Proctitis | Alveolar Capillary Dysplasia | Hereditary Spherocytosis | Desbuquois Syndrome | Takenouchi-Kosaki Syndrome | Diastrophic Dysplasia | Leiomyosarcoma | Chromosome 9q34.3 Deletion Syndrome | Myelomeningocele | Neurodegeneration With Brain Iron Accumulation | Carcinoid Tumor | Syndactyly | Myasthenia | Rash | Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive 1 | Optic Atrophy 2 | Pneumoconiosis | Myopia | Pseudoachondroplasia | Craniolenticulosutural Dysplasia | Insulin Resistance | Urolithiasis | Angioedema | DNA Ligase IV Deficiency | Thin Basement Membrane Disease | Subacute Sclerosing Panencephalitis | Uremic Pruritus | Pemphigus Foliaceus | Hypodontia | Hypophosphatasia | Hypercholesterolemia | Stromal Corneal Dystrophy | Ileitis | Charcot-Marie-Tooth Disease Type 2E | Diabetes Insipidus | Epithelioid Hemangioma | Congenital Afibrinogenemia | HELLP Syndrome | Spinocerebellar Ataxia Type 12 | Tinea Versicolor | Sensory Ataxic Neuropathy, Dysarthria, And Ophthalmoparesis | Barakat Syndrome | Microtia | Pulmonary Alveolar Proteinosis | Osteonecrosis Of The Jaw | Cervicitis | Periventricular Leukomalacia | Methemoglobinemia Type IV | Diffuse Palmoplantar Keratoderma | Spondylocostal Dysostosis | Rheumatoid Arthritis | Aplastic Anemia | Cheilitis | Chylomicron Retention Disease | Anxiety Disorders | Vitamin B12 Deficiency | Presbycusis | Pneumococcal Meningitis | High Molecular Weight Kininogen Deficiency | Headache | Otopalatodigital Syndrome Type 2 | Tay-Sachs Disease | Succinic Semialdehyde Dehydrogenase Deficiency | Genitopatellar Syndrome | Palmoplantar Keratoderma | Cardiomyopathy, Dilated, 1L | Chromosome 17q21.31 Deletion Syndrome | Poirier-Bienvenu Neurodevelopmental Syndrome | Craniofacial Dysostosis | Papilledema | Wilson's Disease | Hyperglycemia | Hyperlipidemia Type V | Lymphopenia | Long QT Syndrome Type 2 | Coronary Artery Disease | Paget's Disease Of The Breast | Retinoblastoma | Acrodysostosis | Potocki-Shaffer Syndrome | Sleep Apnea, Central | Alstrom Syndrome | Miyoshi Myopathy | Kabuki Syndrome 2 | 3-methylglutaconic Aciduria Type IV | Early Infantile Epileptic Encephalopathy | Urea Cycle Disorder | Charcot-Marie-Tooth Disease, Type 2C | Glycogen Storage Disease Type 0, Muscle | Coloboma | Aarskog-Scott Syndrome | Choroideremia | Osteomalacia | Hypothalamic Obesity | Hydrops Fetalis | Tularemia | Desmosterolosis | Juvenile Xanthogranuloma | Bare Lymphocyte Syndrome | Scleroderma | Erythema Multiforme | Migraine | Strabismus | Usher Syndrome | Diabetes | Familial Mediterranean Fever | Pouchitis | Neovascular Glaucoma | AIDS | Withdrawal Syndrome | Pain | Vici Syndrome | Pyoderma Gangrenosum | Lipodystrophy | Oligoasthenoteratozoospermia | Malignant Peripheral Nerve Sheath Tumor | Myoclonic Epilepsy With Ragged Red Fibers | Neuropathy | Microvillus Inclusion Disease | Delirium | Congenital Dyserythropoietic Anemia Type 4 | Smoldering Myeloma | Mitochondrial Encephalomyopathy | Gyrate Atrophy Of The Choroid And Retina | Leber Congenital Amaurosis | Sotos Syndrome | Eosinophilia | Gallstones | Pulmonary Veno-occlusive Disease | Obsessive-compulsive Disorder | Vertigo | Hydrocephalus | Acute Kidney Injury | Adenomatoid Tumor | T-cell Prolymphocytic Leukemia | Acrodermatitis Enteropathica | Cockayne Syndrome | Neuromuscular Disorders | Mitochondrial Myopathy | Hydrolethalus Syndrome | Myositis | Globozoospermia | Prolactinoma | Waardenburg Syndrome Type 4 | Blue Nevus | Histoplasmosis | Hypertension | Pitt-Hopkins Syndrome | Agnathia-Otocephaly Complex | Thalassemia, Beta | Vitreoretinal Degeneration, Snowflake Type | DRESS Syndrome | Urticaria | FG Syndrome | Oculodentodigital Dysplasia | Waardenburg Syndrome Type 1 | Leprosy | Sjogren Syndrome | Lesch-Nyhan Syndrome | Sarcoidosis | Hemangioma | Leukocyte Adhesion Deficiency Type 1 | Kaposi Sarcoma | Adult Polyglucosan Body Disease | Spitz Nevus | Corneal Dystrophy | Exostoses | Anorexia Nervosa | Melanoma | Pre-eclampsia | Glomerulonephritis | Best Macular Dystrophy | Epidermolysis Bullosa Simplex, Dowling-Meara Type | Fibrosarcoma | Diffuse Mesangial Sclerosis | Fontaine Progeroid Syndrome | Herpes Genitalis | Gliosarcoma | Encephalopathy, Ethylmalonic | Unverricht-Lundborg Syndrome | Asthma, Exercise-induced | Autonomic Neuropathy | Pseudohermaphroditism | Usher Syndrome Type I | Pearson Syndrome | Diabetes Type 2 | Metaphyseal Chondrodysplasia, Schmid Type | Spondylometaphyseal Dysplasia | Chronic Thromboembolic Pulmonary Hypertension | Left Ventricular Noncompaction | 3-methylglutaconic Aciduria Type I | Melanoma, Malignant | Hyperparathyroidism-jaw Tumor Syndrome | Dwarfism | Congenital Primary Aphakia | Rubinstein-Taybi Syndrome | Neuroleptic Malignant Syndrome | Hemorrhagic Disorders | Nemaline Myopathy 10 | Multiple Sclerosis | Holoprosencephaly | LEOPARD Syndrome | Angelman Syndrome | Facioscapulohumeral Muscular Dystrophy | Charcot-Marie-Tooth Disease, Type 2 | Acute Anterior Uveitis | Occipital Neuralgia | Fucosidosis | Hereditary Hemorrhagic Telangiectasia Type 2 | Hemolytic Uremic Syndrome, Atypical | Renal Tubular Acidosis | Cancer, Colon | ACTH-independent Macronodular Adrenal Hyperplasia | Schizoaffective Disorder | Chordoid Glioma | Congenital Tufting Enteropathy | Alazami Syndrome | Steel Syndrome | Spinocerebellar Ataxia Type 21 | Episodic Ataxia Type 2 | Pierpont Syndrome | Chudley-McCullough Syndrome | Mucolipidosis Type IV | Hepatitis A | Hypercalciuria | Infantile Spasm | Autoimmune Disease | Macular Degeneration | Motor Neuron Diseases | Hemorrhoids | Lassa Fever | Evans Syndrome | Mitochondrial Cytopathy | Porphyria, Acute Intermittent | Galactosemia | Hypophosphatemic Rickets With Hypercalciuria, Hereditary | Androgenic Alopecia | Takayasu's Arteritis | Brachydactyly | Heterotopic Ossification | Intestinal Tuberculosis | Hypertrophy | Sporadic Hemiplegic Migraine | Impetigo | Intellectual Disability, Autosomal Dominant 5 | Marfan Syndrome | Hereditary Inclusion Body Myopathy | Conduct Disorder | Anterior Segment Dysgenesis | Familial Isolated Hyperparathyroidism | Benign Recurrent Intrahepatic Cholestasis 1 | Lymphoma, Follicular | Spondyloarthritis | Wieacker-Wolff Syndrome | Giant Cell Glioblastoma | Rift Valley Fever | Echinococcosis | Heimler Syndrome | Bulimia Nervosa | Osteogenesis Imperfecta Type I | Pneumonia, Mycoplasma | Kohlschutter-Tonz Syndrome | Hypolipoproteinemia | Basal Ganglia Cerebrovascular Disease | Vascular Cognitive Impairment | Keloid | Familial Partial Lipodystrophy | Acquired Partial Lipodystrophy | Chromosome 16p11.2 Deletion Syndrome | Hypotonia-cystinuria Syndrome | Histiocytosis | Cone Dystrophy | Enterocolitis, Necrotizing | Reflex Epilepsy | Colon Adenoma | Frontotemporal Dementia | Mitochondrial DNA Depletion Syndrome, Hepatocerebral Form | Wolff-Parkinson-White Syndrome | Sleep Apnea, Obstructive | Diabetes Insipidus, Nephrogenic | Congenital Fiber-type Disproportion Myopathy | Marinesco-Sjogren Syndrome | HIBCH Deficiency | Kernicterus | Blue Rubber Bleb Nevus Syndrome | Vogt-Koyanagi-Harada Syndrome | Hereditary Hemorrhagic Telangiectasia | Esotropia | Medium-chain Acyl-CoA Dehydrogenase Deficiency | Familial Male-limited Precocious Puberty | Pituitary Disorders | Hemolytic Uremic Syndrome | Ectopia Lentis, Isolated, Autosomal Recessive | Metanephric Adenoma | X-linked Sideroblastic Anemia | Neurodevelopmental Disorder With Central Hypotonia And Dysmorphic Facies | Salla Disease | Silicosis | Placenta Previa | Anencephaly | Alpers Syndrome | Partington Syndrome | Carpenter Syndrome | N-acetylglutamate Synthase Deficiency | Mitochondrial DNA Depletion Syndrome 13 | Perivascular Epithelioid Cell Tumor | Von Willebrand Disease | Gangliosidosis | Greenberg Dysplasia | Chronic Granulomatous Disease | Epicondylitis | Dysmorphophobia | Facioscapulohumeral Muscular Dystrophy Type 2 | Acromegaly | Vitamin D Deficiency | CDKL5 Deficiency Disorder | Sandhoff Disease | Hypomyelination With Atrophy Of Basal Ganglia And Cerebellum | Dystonia Musculorum Deformans | Teratozoospermia | Progressive External Ophthalmoplegia | Ovarian Hyperstimulation Syndrome | Photosensitivity | Combined Deficiency Of Factor V And Factor VIII | Varices | Primary Hyperoxaluria | Hyperuricemic Nephropathy, Familial Juvenile | Hyperparathyroidism, Primary | Multisystemic Smooth Muscle Dysfunction Syndrome | Li-Fraumeni Syndrome | Congenital Adrenal Hyperplasia | Coronary Heart Disease | Varicocele | Glioblastoma | Pituitary Stalk Interruption Syndrome | Corneal Dystrophies, Hereditary | Retinopathy, Diabetic | C3 Glomerulonephritis | Familial Hypertrophic Cardiomyopathy | Vitiligo